Study Coordinator

UCSF • San Francisco, CA

10h • $79,000 - $84,000

About The Position

The role of the Research Compliance Analyst 2 (internal title: Study Administrator) is to assist the study team and investigators with research activities in locations worldwide. The incumbent will be expected to assist the team in preparing for study implementation, including refining study protocols, obtaining regulatory and ethical approvals, and performing remote and in-person site visits. They will also assist with grant and manuscript writing, and data management/analysis such as designing data collection forms, data cleaning, and participating in data analysis. This individual will monitor adherence to the study protocol across study sites, and serve as a liaison to study personnel at enrollment sites. This individual will also help prepare monitoring reports for the NIH and Data Safety Monitoring Committees. This position will also involve management of study funds across all sites. Using research compliance concepts, applies organization policies and procedures to review and / or pre-review moderately complex, minimal risk research protocols. Works independently in most cases without a great deal of supervision or oversight for routine or standard assignments. Occasionally pre-reviews or highlights potential issues of concern for department head or full committee to consider in their review of research protocols that qualify for full committee review. The Francis I. Proctor Foundation for Research in Ophthalmology at UCSF is committed to engaging in research activities and providing state-of-the-art patient care that address infectious and inflammatory disease that cause blindness. The mission is the prevention of blindness worldwide through research and teaching focused on infectious and inflammatory eye disease.

Requirements

• Staffing, administering or managing research oversight and compliance committee activities related to research activities such as human subjects, animal use and care, conflict of interest and export control.
• Reviews research protocols for use in specific fields.
• Assists in writing and reviewing protocols.
• Ensures compliance with federal, state, and University mandated laws, regulations and policies.

Responsibilities

• Assist the study team and investigators with research activities in locations worldwide.
• Assist the team in preparing for study implementation, including refining study protocols, obtaining regulatory and ethical approvals, and performing remote and in-person site visits.
• Assist with grant and manuscript writing, and data management/analysis such as designing data collection forms, data cleaning, and participating in data analysis.
• Monitor adherence to the study protocol across study sites.
• Serve as a liaison to study personnel at enrollment sites.
• Help prepare monitoring reports for the NIH and Data Safety Monitoring Committees.
• Manage study funds across all sites.
• Apply organization policies and procedures to review and / or pre-review moderately complex, minimal risk research protocols.
• Pre-review or highlight potential issues of concern for department head or full committee to consider in their review of research protocols that qualify for full committee review.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed